Clinical Trial Physician

#hiring. Know anyone who might be interested?

"Remote Opportunity"

Veeda Lifesciences is seeking a passionate "Clinical Trail Physician".

Position Summary:

The Clinical Trial Physician is responsible for providing medical input within the organization as well as to external partners and performing medical review tasks within the context of clinical trials. Furthermore, the Clinical Trial Physician is responsible for undertaking scientific/medical writing tasks within the organization.

Main Duties & Responsibilities:

- Is responsible for the development of:

• All study related documents that fall under the Clinical Science Department scope (e.g., Study Protocols, ICFs - in collaboration with other departments e.g., Clinical Operations, Regulatory, as required -, Pharmacy Manuals, Medical Review Plans, etc.),
• Scientific presentations and manuscripts,
• Medical training material (i.e. therapeutic area and study protocol training material)

1. Delivers internal and external study protocol and therapeutic area training courses
2. Provides medical expertise and consultation within the Company on key therapeutic areas of the clinical development program
3. Provides guidance to all involved departments on the medical and scientific aspects of the assigned clinical trials/projects.
4. Responds to medical queries from all involved parties in assigned clinical trials (e.g., CRAs, Project Managers, Clinical Operations Managers, Investigators) and collaborates with all concerned staff in maintaining an up-to-date study-specific Q&A log
5. Is available 24/7 to respond to urgent medical/protocol related issues derived from an Investigational Site, as applicable
6. Performs periodic medical review of the data from clinical trials according to the study-specific Medical Review Plan requirements (e.g., review of eligibility, review of efficacy and safety data).
7. Performs real-time medical review on urgent medical and safety issues, as needed
8. Collaborates with and provides medical input to the Data Management staff to ensure the successful development of the study-specific eCRF
9. Attends Investigator Meetings and Conferences, as applicable
10. Complies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection and ICH GCP requirements

Professional Experience Requirements:

- Preferred: Clinical experience in the therapeutic area of the assigned study or of the Companys clinical development program

- Preferred: 1 year of experience in a CRO or in the pharma industry in a relevant role (Clinical, Medical Information, Medical Affairs or PV)

Education Requirements:

− Required: Medical Degree

− Preferred: MSc or PhD or Acquired Specialization